Canonical Allele Identifier: CA407041527

Gene: KLK4

Linked Data

• MyVariant Identifiers: chr19:g.51411920G>C (hg19) ; chr19:g.50908664G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.50908664G>C , CM000681.2:g.50908664G>C	GRCh38
NC_000019.9:g.51411920G>C , CM000681.1:g.51411920G>C	GRCh37
NC_000019.8:g.56103732G>C	NCBI36
NG_012154.2:g.7075C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000324041.6:c.390C>G MANE Select	ENSP00000326159.1:p.Asp130Glu
ENST00000324041.5:c.390C>G	ENSP00000326159.1:p.Asp130Glu
ENST00000431178.2:c.243C>G	ENSP00000399448.2:p.Asp81Glu
ENST00000593885.1:c.105C>G	ENSP00000469769.1:p.Asp35Glu
ENST00000596876.1:n.309C>G
ENST00000598305.5:c.105C>G	ENSP00000469963.1:p.Asp35Glu
ENST00000599865.5:n.243C>G
ENST00000602148.1:c.402C>G	ENSP00000472091.1:n.402C>G
NM_001302961.1:c.105C>G	NP_001289890.1:p.Asp35Glu
NM_004917.4:c.390C>G	NP_004908.4:p.Asp130Glu
NR_126566.1:n.383C>G
XM_005259441.3:c.105C>G	XP_005259498.2:p.Asp35Glu
XM_011527545.1:c.390C>G	XP_011525847.1:p.Asp130Glu
XM_011527546.1:c.390C>G	XP_011525848.1:p.Asp130Glu
XM_011527547.1:c.243C>G	XP_011525849.1:p.Asp81Glu
XM_005259441.4:c.105C>G	XP_005259498.2:p.Asp35Glu
XM_011527545.3:c.390C>G	XP_011525847.1:p.Asp130Glu
XM_011527546.2:c.390C>G	XP_011525848.1:p.Asp130Glu
NM_001302961.2:c.105C>G	NP_001289890.1:p.Asp35Glu
NR_126566.2:n.383C>G
NM_004917.5:c.390C>G MANE Select	NP_004908.4:p.Asp130Glu